Transcriptome analysis reveals a dynamic and differential transcriptional response to sulforaphane in normal and prostate cancer cells and suggests a role for Sp1 in chemoprevention

被引:27
作者
Beaver, Laura M. [1 ,2 ]
Buchanan, Alex [2 ,3 ]
Sokolowski, Elizabeth I. [2 ]
Riscoe, Allison N. [2 ]
Wong, Carmen P. [1 ,2 ]
Chang, Jeff H. [3 ,4 ]
Loehr, Christiane V. [5 ]
Williams, David E. [1 ,2 ,4 ]
Dashwood, Roderick H. [1 ,2 ,6 ]
Ho, Emily [1 ,2 ,4 ,7 ]
机构
[1] Oregon State Univ, Linus Pauling Inst, Corvallis, OR 97331 USA
[2] Oregon State Univ, Corvallis, OR 97331 USA
[3] Oregon State Univ, Dept Bot & Plant Pathol, Corvallis, OR 97331 USA
[4] Oregon State Univ, Ctr Genome Res & Biocomp, Corvallis, OR 97331 USA
[5] Oregon State Univ, Coll Vet Med, Dept Biomed Sci, Corvallis, OR 97331 USA
[6] Texas A&M Hlth Sci Ctr, Inst Biosci & Technol, Ctr Epigenet & Dis Prevent, Houston, TX USA
[7] Oregon State Univ, Moore Family Ctr, Corvallis, OR 97331 USA
关键词
Chemoprevention; Prostate cancer; RNA sequencing; Specificity protein 1; Sulforaphane; HISTONE DEACETYLASE ACTIVITY; GENE-EXPRESSION PROFILES; ISOTHIOCYANATE SULFORAPHANE; CRUCIFEROUS VEGETABLES; ANDROGEN RECEPTOR; CYCLE ARREST; INHIBITION; 3,3'-DIINDOLYLMETHANE; INDOLE-3-CARBINOL; PROMOTER;
D O I
10.1002/mnfr.201400269
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Scope: Epidemiological studies provide evidence that consumption of cruciferous vegetables, like broccoli, can reduce the risk of cancer development. Sulforaphane (SFN) is a phytochemical derived from cruciferous vegetables that induces anti-proliferative and pro-apoptotic responses in prostate cancer cells, but not in normal prostate cells. The mechanisms responsible for this cancer-specific cytotoxicity remain unclear. Methods and results: We utilized RNA sequencing and determined the transcriptomes of normal prostate epithelial cells, androgen-dependent prostate cancer cells, and androgen-independent prostate cancer cells treated with SFN. SFN treatment dynamically altered gene expression and resulted in distinct transcriptome profiles depending on prostate cell line. SFN also down-regulated the expression of genes that were up-regulated in prostate cancer cells. Network analysis of genes altered by SFN treatment revealed that the transcription factor Specificity protein 1 (Sp1) was present in an average of 90.5% of networks. Sp1 protein was significantly decreased by SFN treatment in prostate cancer cells and Sp1 may be an important mediator of SFN-induced changes in expression. Conclusion: Overall, the data show that SFN alters gene expression differentially in normal and cancer cells with key targets in chemopreventive processes, making it a promising dietary anti-cancer agent.
引用
收藏
页码:2001 / 2013
页数:13
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